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        <rdf:type rdf:resource="http://www.w3.org/2002/07/owl#TransitiveProperty"/>
        <rdfs:label>has material basis in germline mutation in</rdfs:label>
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        <rdfs:label>disease has feature</rdfs:label>
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    <!-- http://identifiers.org/hgnc/4274 -->

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        <rdfs:label>GJA1</rdfs:label>
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        <rdfs:label>Increased bone mineral density</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0005328 -->

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        <rdfs:label>eye disorder</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0008111 -->

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        <rdfs:label>oculodentodigital dysplasia</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0005328"/>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0015160"/>
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                <someValuesFrom rdf:resource="http://purl.obolibrary.org/obo/HP_0011001"/>
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        </rdfs:subClassOf>
        <ns5:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/4948</ns5:IAO_0000233>
        <ns5:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/6751</ns5:IAO_0000233>
        <rdfs:seeAlso rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://rarediseases.info.nih.gov/diseases/7239/oculodentodigital-dysplasia</rdfs:seeAlso>
        <ns3:curated_content_resource rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://www.malacards.org/card/oculodentodigital_dysplasia</ns3:curated_content_resource>
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        <oboInOwl:hasExactSynonym>Meyer-Schwickerath syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>NORD:1519</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MESH:C563160</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>Orphanet:2710</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>SCTID:38215007</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>oculo-dento-digital syndrome</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasExactSynonym>oculodentodigital dysplasia</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>DOID:0060291</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>Oculo-Dento-Digital Dysplasia</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>UMLS:C0812437</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>oculodentoosseous dysplasia</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>oculo-dento-digital dysplasia</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>ICD9:759.89</oboInOwl:hasDbXref>
        <ns5:IAO_0000115>Oculodentodigital dysplasia (ODDD) is characterized by craniofacial, neurologic, limb and ocular abnormalities.</ns5:IAO_0000115>
        <oboInOwl:hasRelatedSynonym>oculodentodigital syndrome</oboInOwl:hasRelatedSynonym>
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        <oboInOwl:hasDbXref>GARD:0007239</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>ODDD syndrome</oboInOwl:hasExactSynonym>
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        <oboInOwl:hasRelatedSynonym>ODDD</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasExactSynonym>odd syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>MedDRA:10063691</oboInOwl:hasDbXref>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0015160 -->

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        <rdfs:label>multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0018230 -->

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        <rdfs:label>skeletal dysplasia</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0019287 -->

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        <rdfs:label>ectodermal dysplasia syndrome</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0019703 -->

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        <rdfs:label>obsolete primary bone dysplasia with increased bone density</rdfs:label>
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